Wriessnegger Tamara, Augustin Peter, Engleder Matthias, Leitner Erich, Müller Monika, Kaluzna Iwona, Schürmann Martin, Mink Daniel, Zellnig Günther, Schwab Helmut, Pichler Harald
ACIB-Austrian Centre of Industrial Biotechnology, Petersgasse 14, 8010 Graz, Austria.
Institute of Molecular Biotechnology, Graz University of Technology, Petersgasse 14/2, 8010 Graz, Austria.
Metab Eng. 2014 Jul;24:18-29. doi: 10.1016/j.ymben.2014.04.001. Epub 2014 Apr 16.
The sesquiterpenoid (+)-nootkatone is a highly demanded and highly valued aroma compound naturally found in grapefruit, pummelo or Nootka cypress tree. Extraction of (+)-nootkatone from plant material or its production by chemical synthesis suffers from low yields and the use of environmentally harmful methods, respectively. Lately, major attention has been paid to biotechnological approaches, using cell extracts or whole-cell systems for the production of (+)-nootkatone. In our study, the yeast Pichia pastoris initially was applied as whole-cell biocatalyst for the production of (+)-nootkatone from (+)-valencene, the abundant aroma compound of oranges. Therefore, we generated a strain co-expressing the premnaspirodiene oxygenase of Hyoscyamus muticus (HPO) and the Arabidopsis thaliana cytochrome P450 reductase (CPR) that hydroxylated extracellularly added (+)-valencene. Intracellular production of (+)-valencene by co-expression of valencene synthase from Callitropsis nootkatensis resolved the phase-transfer issues of (+)-valencene. Bi-phasic cultivations of P. pastoris resulted in the production of trans-nootkatol, which was oxidized to (+)-nootkatone by an intrinsic P. pastoris activity. Additional overexpression of a P. pastoris alcohol dehydrogenase and truncated hydroxy-methylglutaryl-CoA reductase (tHmg1p) significantly enhanced the (+)-nootkatone yield to 208mg L(-1) cell culture in bioreactor cultivations. Thus, metabolically engineered yeast P. pastoris represents a valuable, whole-cell system for high-level production of (+)-nootkatone from simple carbon sources.
倍半萜类化合物(+)-诺卡酮是一种需求量大且价值高的香气化合物,天然存在于葡萄柚、文旦或诺特卡扁柏中。从植物材料中提取(+)-诺卡酮或通过化学合成生产该化合物,分别存在产率低和使用对环境有害方法的问题。最近,人们主要关注生物技术方法,即使用细胞提取物或全细胞系统来生产(+)-诺卡酮。在我们的研究中,最初将酵母毕赤酵母用作全细胞生物催化剂,以从(+)-瓦伦烯生产(+)-诺卡酮,(+)-瓦伦烯是橙子中丰富的香气化合物。因此,我们构建了一个共表达天仙子的前马螺二烯氧化酶(HPO)和拟南芥细胞色素P450还原酶(CPR)的菌株,该菌株可将细胞外添加的(+)-瓦伦烯羟基化。通过共表达来自诺特卡柳杉的瓦伦烯合酶在细胞内生产(+)-瓦伦烯,解决了(+)-瓦伦烯的相转移问题。毕赤酵母的双相培养产生了反式诺卡醇,并通过毕赤酵母的固有活性将其氧化为(+)-诺卡酮。额外过表达毕赤酵母醇脱氢酶和截短的羟甲基戊二酰辅酶A还原酶(tHmg1p),在生物反应器培养中显著提高了(+)-诺卡酮产量,达到208mg L(-1)细胞培养物。因此,经过代谢工程改造的酵母毕赤酵母是一种有价值的全细胞系统,可从简单碳源高效生产(+)-诺卡酮。